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[3] [10] Classification [edit] Idiopathic pulmonary fibrosis (IPF) belongs to a large group of more than 200 lung diseases known as interstitial lung diseases (ILDs), which are characterized by the involvement of the lung interstitium, [10] the tissue between the air sacs of the lung

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This possibility warrants further investigation in a larger cohort

This vital peptide supports detoxification pathways, boosts immune function, and promotes respiratory and neurological wellness